D-Cycloserine for the Treatment of Chronic, Refractory Low Back Pain

Abstract

Chronic low back pain constitutes the major form of chronic pain, with a prevalence as high as 70-85% in adults at some timein their lives. This 26-week, double blind, randomized, placebo controlled two-arm parallel-group study will evaluate 244participants to determine if treatment with d-cycloserine in individuals with chronic, refractory low back pain will demonstrategreater reduction in pain compared to individuals treated with placebo. After a two-week screening period, individuals arerandomized to receive either 12 weeks of d-cycloserine or placebo and then followed for an additional 12 weeks to evaluatepersistence of benefit at study endpoint, 24 weeks after randomization. Follow-up visits and data collection will occur atbaseline and 2, 6, 12, and 24 weeks after randomization to assess general health, pain, proper treatment use, and sideeffects. Pain and safety will also be assessed at 16 and 20 weeks after randomization by phone calls.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2022
Accession Number
AD1199692

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  • Thoams J. Schnitzer

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  • Northwestern University

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